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dc.contributor.authorLozano-Ojalvo, Danieles_ES
dc.contributor.authorCamara, Carmenes_ES
dc.contributor.authorLopez-Granados, Eduardoes_ES
dc.contributor.authorNozal, Pilares_ES
dc.contributor.authorDel Pino-Molina, Lucíaes_ES
dc.contributor.authorBravo-Gallego, Luz Yadiraes_ES
dc.contributor.authorPaz-Artal, Estelaes_ES
dc.contributor.authorPion, Marjoriees_ES
dc.contributor.authorCorrea-Rocha, Rafaeles_ES
dc.contributor.authorOrtiz, Albertoes_ES
dc.contributor.authorLópez Hoyos, Marcos es_ES
dc.contributor.authorIribarren, Marta Erroes_ES
dc.contributor.authorPortoles, Josees_ES
dc.contributor.authorRojo-Portoles, Maria Pilares_ES
dc.contributor.authorOjeda, Gloriaes_ES
dc.contributor.authorCervera, Isabeles_ES
dc.contributor.authorGonzalez-Perez, Mariaes_ES
dc.contributor.authorBodega-Mayor, Irenees_ES
dc.contributor.authorMontes-Casado, Mariaes_ES
dc.contributor.authorPortoles, Pilares_ES
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2022-05-16T15:04:15Z
dc.date.available2022-05-16T15:04:15Z
dc.date.issued2021es_ES
dc.identifier.issn2211-1247es_ES
dc.identifier.urihttp://hdl.handle.net/10902/24842
dc.description.abstractThe rapid development of mRNA-based vaccines against the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) led to the design of accelerated vaccination schedules that have been extremely effective in naive individuals. While a two-dose immunization regimen with the BNT162b2 vaccine has been demonstrated to provide a 95% efficacy in naive individuals, the effects of the second vaccine dose in individuals who have previously recovered from natural SARS-CoV-2 infection has not been investigated in detail. In this study, we characterize SARS-CoV-2 spike-specific humoral and cellular immunity in naive and previously infected individuals during and after two doses of BNT162b2 vaccination. Our results demonstrate that, while the second dose increases both the humoral and cellular immunity in naive individuals, COVID-19 recovered individuals reach their peak of immunity after the first dose. These results suggests that a second dose, according to the current standard regimen of vaccination, may be not necessary in individuals previously infected with SARS-CoV-2.es_ES
dc.description.sponsorshipFunding: Research reported in this publication was supported in part by the National Cancer Institute of the NIH (5R01HD102614-02; R01CA249204 and R01CA248984) and an ISMMS seed fund to E.G. The authors gratefully acknowledge use of the services and facilities of the Tisch Cancer Institute supported by a NCI Cancer Center Support Grant (P30 CA196521). M.S. was supported by a NCI training grant (T32CA078207). This work was supported by an ISMMS seed fund to J.O.; Instituto de Salud Carlos III (COV20-00668) to R.C.R.; the Instituto de Salud Carlos III, Spanish Ministry of Science and Innovation (COVID-19 research call COV20/00181) co-financed by the European Development Regional Fund ‘‘A way to achieve Europe’’ to E.P.; the Instituto de Salud Carlos III, Spain (COV20/00170); the Government of Cantabria, Spain (2020UIC22-PUB-0019) to M.L.H.; the Instituto de Salud Carlos III (PI16CIII/00012) to P.P.; the Fondo Social Europeo e Iniciativa de Empleo Juvenil YEI (Grant PEJ2018-004557-A) to M.P.E.; and by REDInREN 016/009/009 ISCIII. This project has received funding from the European Union Horizon 2020 research and innovation programs VACCELERATE and INsTRuCT under grant agreements 101037867 and 860003.es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherCell Press Elsevieres_ES
dc.rightsAttribution 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/*
dc.sourceCell Rep . 2021 Aug 24;36(8):109570es_ES
dc.titleDifferential effects of the second SARS-CoV-2 mRNA vaccine dose on T cell immunity in naive and COVID-19 recovered individualses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1016/j.celrep.2021.109570es_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1016/j.celrep.2021.109570es_ES
dc.type.versionpublishedVersiones_ES


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Attribution 4.0 InternationalExcepto si se señala otra cosa, la licencia del ítem se describe como Attribution 4.0 International